Molecular Model of the Human 26S Proteasome

被引:189
作者
da Fonseca, Paula C. A. [1 ]
He, Jun [1 ]
Morris, Edward P. [1 ]
机构
[1] Inst Canc Res, Chester Beatty Labs, Div Struct Biol, London SW3 6JB, England
关键词
REGULATORY PARTICLE; 20S PROTEASOME; CRYSTAL-STRUCTURE; UBIQUITIN RECEPTORS; STRUCTURAL INSIGHTS; COP9; SIGNALOSOME; DEGRADATION; DOMAIN; ACTIVATION; REVEALS;
D O I
10.1016/j.molcel.2012.03.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The 26S proteasome plays a fundamental role in eukaryotic homeostasis by undertaking the highly controlled degradation of a wide range of proteins, including key cellular regulators such as those controlling cell-cycle progression and apoptosis. Here we report the structure of the human 26S proteasome determined by cryo-electron microscopy and single-particle analysis, with secondary structure elements identified both in the 20S proteolytic core region and in the 19S regulatory particle. We have used this information together with crystal structures, homology models, and other biochemical information to construct a molecular model of the complete 26S proteasome. This model allows for a detailed description of the 20S core within the 26S proteasome and redefines the overall assignment of subunits within the 19S regulatory particle. The information presented here provides a strong basis for a mechanistic understanding of the 26S proteasome.
引用
收藏
页码:54 / 66
页数:13
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